Molla Akhteruzzaman, Mo Hongmei, Vasavanonda Sudthida, Han Lixin, Lin C Thomas, Hsu Ann, Kempf Dale J
Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, Illinois 60064, USA.
Antimicrob Agents Chemother. 2002 Jul;46(7):2249-53. doi: 10.1128/AAC.46.7.2249-2253.2002.
The in vitro inhibition of wild-type human immunodeficiency virus (HIV) by combinations of lopinavir and six other protease inhibitors over a range of two-drug combination ratios was evaluated. Combinations of lopinavir with indinavir, nelfinavir, amprenavir, tipranavir, and BMS-232632 generally displayed an additive relationship. In contrast, a consistent, statistically significant synergistic inhibition of HIV type 1 replication with combinations of lopinavir and saquinavir was observed. Analysis of the combination indices indicated that lopinavir with saquinavir was synergistic over the entire range of drug combination ratios tested and at all levels of inhibition in excess of 40%. Cellular toxicity was not observed at the highest drug concentrations tested. These results suggest that administration of combinations of the appropriate dose of lopinavir with other protease inhibitors in vivo may result in enhanced antiviral activity with no associated increase in cellular cytotoxicity. More importantly, the observed in vitro synergy between lopinavir and saquinavir provides a theoretical basis for the clinical exploration of a novel regimen of lopinavir-ritonavir and saquinavir.
评估了洛匹那韦与其他六种蛋白酶抑制剂在一系列两药组合比例下对野生型人类免疫缺陷病毒(HIV)的体外抑制作用。洛匹那韦与茚地那韦、奈非那韦、安普那韦、替拉那韦和BMS-232632的组合通常呈现相加关系。相比之下,观察到洛匹那韦与沙奎那韦的组合对1型HIV复制具有一致的、统计学上显著的协同抑制作用。组合指数分析表明,在测试的整个药物组合比例范围内以及超过40%的所有抑制水平下,洛匹那韦与沙奎那韦均具有协同作用。在测试的最高药物浓度下未观察到细胞毒性。这些结果表明,在体内给予适当剂量的洛匹那韦与其他蛋白酶抑制剂组合可能会增强抗病毒活性,而不会伴随细胞细胞毒性增加。更重要的是,观察到的洛匹那韦与沙奎那韦之间的体外协同作用为洛匹那韦-利托那韦和沙奎那韦新方案的临床探索提供了理论基础。